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The Journal of Allergy and Clinical Immunology
|
September 27, 2020
Coronavirus disease 2019 in patients with inborn errors of immunity: An international study
Isabelle Meyts, Giorgia Bucciol, Isabella Quinti, et al.
Nature Communications
|
November 27, 2025
Human plasma proteomic profile of clonal hematopoiesis
Zhi Yu, Amélie Vromman, Ngoc Quynh H Nguyen, et al.
American Journal of Human Genetics
|
September 3, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
Linda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
American Journal of Human Genetics
|
August 4, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
Linda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
Nature Communications
|
October 16, 2025
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutations
Joshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Medrxiv : the Preprint Server for Health Sciences
|
October 24, 2023
Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease
Gabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.
American Journal of Human Genetics
|
April 2, 2024
Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease
Gabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 3, 2024
Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood
Yasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, et al.
American Journal of Human Genetics
|
January 14, 2025
Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood
Yasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 8, 2024
Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis
Monica H Wojcik, Gabrielle Lemire, Maha S Zaki, et al.
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of 24
Search research articles
Search
Showing results (221-230 of 240) with videos related to
Sort By:
Page
of 24
The Journal of Allergy and Clinical Immunology
|
September 27, 2020
Coronavirus disease 2019 in patients with inborn errors of immunity: An international study
Isabelle Meyts, Giorgia Bucciol, Isabella Quinti, et al.
Nature Communications
|
November 27, 2025
Human plasma proteomic profile of clonal hematopoiesis
Zhi Yu, Amélie Vromman, Ngoc Quynh H Nguyen, et al.
American Journal of Human Genetics
|
September 3, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
Linda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
American Journal of Human Genetics
|
August 4, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
Linda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
Nature Communications
|
October 16, 2025
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutations
Joshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Medrxiv : the Preprint Server for Health Sciences
|
October 24, 2023
Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease
Gabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.
American Journal of Human Genetics
|
April 2, 2024
Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease
Gabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 3, 2024
Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood
Yasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, et al.
American Journal of Human Genetics
|
January 14, 2025
Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood
Yasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 8, 2024
Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis
Monica H Wojcik, Gabrielle Lemire, Maha S Zaki, et al.
Page
of 24